Hem/Onc Flashcards
How to differentiate between alpha and beta thalassemia
Electrophoresis, beta thalassemia will have increased hemoglobin A2
Dx and Management of HIT
Dx: clinical, definitive test is serotonin release assay
Stop all heparin products
Transition to argatroban or fondaparinux
Start warfarin when platelet count >150,000 and after treatment with another anticoagulant
Findings on EGD of patient with pernicious anemia
Atrophy in the gastric fundus and body (absent rugae)
TTP
Due to acquired antibodies against ADAMTS13
Needs plasma exchange to antibodies and replenish ADAMTS13 levels from donor
CML
Translocation of chromosomes 9 and 22, creates a bcr-abl fusion protein that leads to unregulated stimulation of the tyrosine kinase system
Tx w/ tyrosine kinase inhibitor
Tx for prolonged bleeding time in patients with renal dysfunction
IV desmopressin, works be releasing factor VIII:von Willebrand factor multimers from endothelium
Best treatment for methotrexate induced macrocytic anemia
Folinic acid (leucovorin) rather than folic acid
Vitamin K reversal
Prothrombin complex concentrate (acts within 10min) and vitamin K (takes 12-24h)
Tx of ITP
mild or no bleeding:observe
bleeding: IVIG